ID
12594
Descripción
Study to Assess Hemodynamic Effects, Safety and Tolerability of Chimeric Natriuretic Peptide (CD-NP) in Patients With Stabilized Acute Heart Failure (AHF); ODM derived from: https://clinicaltrials.gov/show/NCT00699712
Link
https://clinicaltrials.gov/show/NCT00699712
Palabras clave
Versiones (1)
- 3/12/15 3/12/15 -
Subido en
3 de diciembre de 2015
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Acute Decompensated Heart Failure NCT00699712
Eligibility Acute Decompensated Heart Failure NCT00699712
- StudyEvent: Eligibility
Descripción
Exclusion criteria
Descripción
administration of intravenous radiographic contrast agent within 7 days prior to screening or planned iv contrast media administration in the 4 days after screening or acute contrast-induced nephropathy at the time of screening
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0742799
- UMLS CUI [2]
- C0268775
Descripción
current or planned treatment with any iv therapies, including diuretics, vasodilators (including nesiritide), vasopressin antagonists, positive inotropic agents and vasopressors, or mechanical support
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2]
- C0348016
Descripción
current or planned ultrafiltration, hemofiltration, or dialysis within 7 days of screening
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0041612
- UMLS CUI [2]
- C0019014
- UMLS CUI [3]
- C0011946
Descripción
significant pulmonary disease
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0024115
Descripción
valvular heart disease
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0018824
Descripción
any organ transplant recipient or patient currently listed for transplant or admitted for any transplantation.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0040732
Descripción
major surgery
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0679637
Descripción
other major disability or disease with expected survival less than 6 months
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0023671
- UMLS CUI [2]
- C0009488
Descripción
major neurologic event, including cerebrovascular events, in the 60 days prior to screening
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0027765
- UMLS CUI [2]
- C0852396
Descripción
clinical diagnosis of acute coronary syndrome within 45 days of screening
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0948089
Descripción
troponin t ≥ 3 times the upper limit of normal at screening
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1141947
Descripción
significant arrhythmias
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0003811
Descripción
cardiomyopathy
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0155686
- UMLS CUI [2]
- C0878544
Descripción
liver dysfunction
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0086565
Descripción
study subject participation status
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2348568
Similar models
Eligibility Acute Decompensated Heart Failure NCT00699712
- StudyEvent: Eligibility
C0268775 (UMLS CUI [2])
C0348016 (UMLS CUI [2])
C0019014 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
C0009488 (UMLS CUI [2])
C0852396 (UMLS CUI [2])
C0878544 (UMLS CUI [2])